syngo.via View&GO (Version VA10A)— 510(k) K182208
Substantially EquivalentSiemens Healthcare GmbH
FDA 510(k) clearance K182208 for syngo.via View&GO (Version VA10A), Substantially Equivalent on 2018-09-07. Applicant: Siemens Healthcare GmbH.
Clearance details
- Applicant
- Siemens Healthcare GmbH
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Forchheim, DE
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.